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Pathway Description
Nicotinic Acetylcholine
Rattus norvegicus
Category:
Metabolite Pathway
Sub-Category:
Physiological
Created: 2023-09-20
Last Updated: 2024-01-21
Nicotinic acetylcholine receptors, or nAChRs, are receptor polypeptides that respond to the neurotransmitter acetylcholine. Nicotinic receptors also respond to drugs such as the agonist nicotine. They are found in the central and peripheral nervous system, muscle, and many other tissues of many organisms. At the neuromuscular junction they are the primary receptor in muscle for motor nerve-muscle communication that controls muscle contraction. In the peripheral nervous system: (1) they transmit outgoing signals from the presynaptic to the postsynaptic cells within the sympathetic and parasympathetic nervous system, and (2) they are the receptors found on skeletal muscle that receive acetylcholine released to signal for muscular contraction. In the immune system, nAChRs regulate inflammatory processes and signal through distinct intracellular pathways. The nicotinic receptors are considered cholinergic receptors, since they respond to acetylcholine. Nicotinic receptors get their name from nicotine which does not stimulate the muscarinic acetylcholine receptors but selectively binds to the nicotinic receptors instead. As ionotropic receptors, nAChRs are directly linked to ion channels. New evidence suggests that these receptors can also use second messengers (as metabotropic receptors do) in some cases. Nicotinic acetylcholine receptors are the best-studied of the ionotropic receptors. Opening of the channel allows positively charged ions to move across it; in particular, sodium enters the cell and potassium exits. The net flow of positively charged ions is inward. The nAChR is a non-selective cation channel, meaning that several different positively charged ions can cross through. The activation of receptors by nicotine modifies the state of neurons through two main mechanisms. On one hand, the movement of cations causes a depolarization of the plasma membrane (which results in an excitatory postsynaptic potential in neurons) leading to the activation of voltage-gated ion channels. On the other hand, the entry of calcium acts, either directly or indirectly, on different intracellular cascades. This leads, for example, to the regulation of activity of some genes or the release of neurotransmitters.
References
Nicotinic Acetylcholine References
Lu B, Kwan K, Levine YA, Olofsson PS, Yang H, Li J, Joshi S, Wang H, Andersson U, Chavan SS, Tracey KJ: alpha7 nicotinic acetylcholine receptor signaling inhibits inflammasome activation by preventing mitochondrial DNA release. Mol Med. 2014 Aug 14;20(1):350-8. doi: 10.2119/molmed.2013.00117.
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Ishii K, Oda Y, Ichikawa T, Deguchi T: Complementary DNAs for choline acetyltransferase from spinal cords of rat and mouse: nucleotide sequences, expression in mammalian cells, and in situ hybridization. Brain Res Mol Brain Res. 1990 Feb;7(2):151-9. doi: 10.1016/0169-328x(90)90092-r.
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Kengaku M, Misawa H, Deguchi T: Multiple mRNA species of choline acetyltransferase from rat spinal cord. Brain Res Mol Brain Res. 1993 Apr;18(1-2):71-6. doi: 10.1016/0169-328x(93)90174-n.
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Wu D, Hersh LB: Identification of an active site arginine in rat choline acetyltransferase by alanine scanning mutagenesis. J Biol Chem. 1995 Dec 8;270(49):29111-6. doi: 10.1074/jbc.270.49.29111.
Pubmed: 7493935
Boulter J, Evans K, Goldman D, Martin G, Treco D, Heinemann S, Patrick J: Isolation of a cDNA clone coding for a possible neural nicotinic acetylcholine receptor alpha-subunit. Nature. 1986 Jan 30-Feb 5;319(6052):368-74. doi: 10.1038/319368a0.
Pubmed: 3753746
Boulter J, Connolly J, Deneris E, Goldman D, Heinemann S, Patrick J: Functional expression of two neuronal nicotinic acetylcholine receptors from cDNA clones identifies a gene family. Proc Natl Acad Sci U S A. 1987 Nov;84(21):7763-7. doi: 10.1073/pnas.84.21.7763.
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Yang X, McDonough J, Fyodorov D, Morris M, Wang F, Deneris ES: Characterization of an acetylcholine receptor alpha 3 gene promoter and its activation by the POU domain factor SCIP/Tst-1. J Biol Chem. 1994 Apr 8;269(14):10252-64.
Pubmed: 8144606
Starr TV, Prystay W, Snutch TP: Primary structure of a calcium channel that is highly expressed in the rat cerebellum. Proc Natl Acad Sci U S A. 1991 Jul 1;88(13):5621-5. doi: 10.1073/pnas.88.13.5621.
Pubmed: 1648226
Yu AS, Hebert SC, Brenner BM, Lytton J: Molecular characterization and nephron distribution of a family of transcripts encoding the pore-forming subunit of Ca2+ channels in the kidney. Proc Natl Acad Sci U S A. 1992 Nov 1;89(21):10494-8. doi: 10.1073/pnas.89.21.10494.
Pubmed: 1279681
Snutch TP, Leonard JP, Gilbert MM, Lester HA, Davidson N: Rat brain expresses a heterogeneous family of calcium channels. Proc Natl Acad Sci U S A. 1990 May;87(9):3391-5. doi: 10.1073/pnas.87.9.3391.
Pubmed: 1692134
Pragnell M, Sakamoto J, Jay SD, Campbell KP: Cloning and tissue-specific expression of the brain calcium channel beta-subunit. FEBS Lett. 1991 Oct 21;291(2):253-8. doi: 10.1016/0014-5793(91)81296-k.
Pubmed: 1657644
Yang L, Katchman A, Morrow JP, Doshi D, Marx SO: Cardiac L-type calcium channel (Cav1.2) associates with gamma subunits. FASEB J. 2011 Mar;25(3):928-36. doi: 10.1096/fj.10-172353. Epub 2010 Dec 2.
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Lundby A, Secher A, Lage K, Nordsborg NB, Dmytriyev A, Lundby C, Olsen JV: Quantitative maps of protein phosphorylation sites across 14 different rat organs and tissues. Nat Commun. 2012 Jun 6;3:876. doi: 10.1038/ncomms1871.
Pubmed: 22673903
Chu PJ, Best PM: Molecular cloning of calcium channel alpha(2)delta-subunits from rat atria and the differential regulation of their expression by IGF-1. J Mol Cell Cardiol. 2003 Feb;35(2):207-15.
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Hatano S, Yamashita T, Sekiguchi A, Iwasaki Y, Nakazawa K, Sagara K, Iinuma H, Aizawa T, Fu LT: Molecular and electrophysiological differences in the L-type Ca2+ channel of the atrium and ventricle of rat hearts. Circ J. 2006 May;70(5):610-4. doi: 10.1253/circj.70.610.
Pubmed: 16636499
This pathway was propagated using PathWhiz -
Pon, A. et al. Pathways with PathWhiz (2015) Nucleic Acids Res. 43(Web Server issue): W552–W559.
Propagated from SMP0121669
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